Search

Your search keyword '"TEKİN, Mustafa"' showing total 1,371 results

Search Constraints

Start Over You searched for: Author "TEKİN, Mustafa" Remove constraint Author: "TEKİN, Mustafa"
1,371 results on '"TEKİN, Mustafa"'

Search Results

52. Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling

53. A How-to Guide to Building a Robust SARS-CoV-2 Testing Program at a University-Based Health System

54. ADAMTSL2 mutations determine the phenotypic severity in Geleophysic Dysplasia

55. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

56. Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents

59. Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development

62. Genetic Landscape of Hearing Loss in the Caribbean: A Narrative Review.

63. Readability of online educational materials for brainstem implants: An assessment.

64. Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism.

65. Two novel heterozygous exonic deletions lead to Chanarin–Dorfman syndrome in a patient with congenital ichthyosis, sensorineural hearing loss, and liver dysfunction.

67. Biallelic CRELD1 variants cause a multisystem syndrome including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.

68. Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

69. Wear behavior of in-situ oxide dispersion strengthened Fe-8Ni alloy with Zr additions

72. HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder

73. De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

75. Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort

76. Novel EYA1 variants causing Branchio-oto-renal syndrome

77. OG-AG ELEKTRİK ŞEBEKELERİNDE DİNAMİK KONTROLLÜ KOMPANZASYON UYGULAMASI

83. MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss

85. Bi-allelic variants in INTS11 are associated with a complex neurological disorder

86. A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network

87. RExPRT: a machine learning tool to predict pathogenicity of tandem repeat loci

88. BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screening

93. ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice

95. BCKDK deficiency: a treatable neurodevelopmental disease amenable to newborn screening

97. P136: Functional studies in ADAMTSL2-related geleophysic dysplasia provide insights into pathogenesis and potential treatment targets*

98. P121: Comparison of diagnostic outcome amongst different ethnic backgrounds in UDN participants at the University of Miami clinical site

99. P642: Diagnostic yield of multi-omics approach in Undiagnosed Diseases Network Miami clinical site

Catalog

Books, media, physical & digital resources